Imaging Clinical Research Scientist
New
J
JobgetherBiotechnology / Pharma
Based in the United StatesFull-TimeSenior
SalaryBase salary range of approximately $177,000–$338,800
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Job Details
- Languages
- English
- Experience
- At least 5 years of clinical development experience, including a minimum of 3 years in an industry environment.
- Required Skills
- GCP
Requirements
- PhD in a relevant scientific or technical discipline.
- At least 5 years of clinical development experience, including a minimum of 3 years in an industry environment.
- Experience with tracer development and/or clinical imaging research.
- Strong scientific knowledge of molecular imaging and experience interpreting PET/CT, SPECT/CT, or related imaging datasets.
- Understanding of imaging biomarkers, patient stratification, disease activity assessment, and longitudinal disease monitoring.
- Familiarity with Good Clinical Practice (GCP) principles and applicable clinical and regulatory requirements.
- Demonstrated ability to lead cross-functional projects and collaborate with internal and external stakeholders.
- Fluency in written and spoken English.
- Willingness to travel approximately 10–15% as required.
Responsibilities
- Lead the design and execution of integrated clinical development programs for diagnostic radiopharmaceuticals across oncology, immunology, cardiovascular disease, and related therapeutic areas.
- Define clinical strategies, endpoints, patient populations, imaging criteria, and study approaches across early- and late-phase development.
- Design and support studies assessing diagnostic accuracy, imaging timing, patient-selection biomarkers, and performance compared with standard-of-care imaging.
- Analyze and interpret molecular imaging data, including tracer biodistribution, tumor localization, dosimetry considerations, longitudinal response, and quantitative imaging biomarkers.
- Lead cross-functional initiatives and coordinate with CROs, academic institutions, technology providers, software developers, and imaging equipment manufacturers.
- Author and review clinical and regulatory materials, including Investigator’s Brochures, protocols, amendments, clinical study reports, regulatory briefing documents, and imaging-related technical documentation.
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